Programmable Arrays

ABSTRACT

Biomolecule arrays on a substrate are described which contain a plurality of biomolecules, such as coding nucleic acids and/or isolated polypeptides, at a plurality of discrete, isolated, locations. The arrays can be used, for example, in high throughput genomics and proteomics for specific uses including, but not limited molecular diagnostics for early detection, diagnosis, treatment, prognosis, monitoring clinical response, and protein crystallography.

CROSS REFERENCE

This application claims priority to U.S. Provisional Patent ApplicationSer. No. 61/551,128 filed Oct. 25, 2011, incorporated by referenceherein in its entirety.

STATEMENT OF GOVERNMENT RIGHTS

This invention was made with government support under grant number R42RR031446 awarded by National Institutes of Health. The government hascertain rights in the invention.

BACKGROUND

Microarrays have revolutionized molecular biology by enabling thousandsof experiments to be performed simultaneously within the size of asingle microscope slide. Originally microarrays consist of thousands ofspots of short nucleotide polymers that are either synthesized directlyonto the microarray surface or pre-synthesized and then spotted onto thesurface. These ‘ oligonucleotide’ microarrays are typically used todetect mRNAs that correspond to gene expression. The field ofmicroarrays has expanded to now include arrays of various differenttypes of biological molecules (biomolecules) such as peptides, siRNA,microRNA, antibodies, or proteins. However many of these emergingmicroarrays have yet to reach their full potential, as research orclinical diagnostic tools, since they are more difficult to manufacturethan oligonucleotide microarrays. For example, currently proteinmicroarrays are typically manufactured by expressing and purifyingthousands of proteins, which are then stored until they are printedusing pin-spotters, a process flow with many inherent logisticalproblems. Furthermore, many proteins are unstable so these steps mustall be maintained at cold temperature. Nucleic Acid Programmable ProteinArrays (NAPPA) is a well-established method that gets around theseproblems. It involves first printing DNA microarrays and thentranscribing and translating the DNA into proteins directly on themicroarray surface. This has many advantages since the DNA arrays arerelatively stable, even at room temperature, and the proteins are oftenexpressed immediately before an experiment so they remain functional.Currently NAPPA array density is limited to several thousand proteinsper array. There are many compelling needs to cost-effectivelymanufacture higher density protein and other types of microarrays.

SUMMARY OF THE INVENTION

In a first aspect, the present invention provides biomolecule arrays,comprising (a) a first substrate; and (b) biomolecules comprising atleast 10 isolated coding nucleic acids and/or at least 10 isolatedpolypeptides, wherein each nucleic acid and/or polypeptide is physicallyconfined at a discrete location on the first substrate, and wherein eachnucleic acid is capable of expressing its encoded product in situ at itsdiscrete location on the substrate, and/or wherein each polypeptide iscapable of a characteristic activity in situ at its discrete location onthe substrate; wherein the discrete locations are separated from eachother on the first substrate by a center to center spacing of betweenabout 20 nm and about 1 mm.

In a second aspect, the present invention provides arrays comprising (a)a silicon-containing substrate, having a surface comprising a pluralityof nanowells at discrete locations wherein the discrete locations areseparated from each other on the silicon-containing substrate by acenter to center spacing of between about 20 nm and about 1 mm; and (b)biomolecules capable of capturing another molecule located at eachdiscrete location. In one embodiment, the silicon-containing substrateis a silica or silicon substrate, such as a glass or a silicon wafer

In one embodiment of either of these aspects, the discrete locations areseparated from each other on the first substrate by a center to centerspacing of between about 20 nm and about 100 μm. In another embodiment,each physically confined discrete location comprises a well. In afurther embodiment, each well has a diameter of between about 14 nm andabout 0.75 mm. In another embodiment, the wells are present on the firstsubstrate at a density of between about 250 billion wells per squarecentimeter and about 100 well per square centimeter. In a still furtherembodiment, the discrete locations are functionalized. In anotherembodiment, each discrete location further comprises reagents forexpressing the encoded nucleic acid product and/or for testingpolypeptide activity. In a further embodiment, each discrete locationfurther comprises reagents for expressing the encoded nucleic acidproduct and/or for testing polypeptide activity and where those reagentsare added to the array separately from the nucleic acids orpolypeptides. In one embodiment, the reagent comprises a reticulocytelysate. In a further embodiment, the biomolecules comprise at least 10isolated coding nucleic acids. In another embodiment, the biomoleculescomprise at least 10 isolated polypeptides. In a further embodiment, thenucleic acids and/or polypeptides are bound to the substrate.

In another embodiment of either of these aspects, either (i) the arrayfurther comprises a capture substrate adapted to mate with the firstsubstrate wherein the capture substrate is functionalized to capture andisolate the expression product; or (ii) the discrete locations arefurther functionalized to capture and isolate the expression product.

In another embodiment of either of these aspects, the biomoleculescomprise antigen or antibodies, and the like. In a further embodiment,the biomolecules are attached to the surface of the first substratethrough a divalent linking group to a functional group capable ofbinding to or associating with the surface of the substrate.

In a third aspect, the present invention provides methods for in situnucleic acid expression, comprising (a) contacting each discretelocation of the array of any embodiment or combination of embodiments ofthe invention with reagents for nucleic acid expression to form amixture; and (b) incubating the mixture under conditions suitable fornucleic acid expression.

In a fourth aspect, the present invention provides methods forexpressing and capturing a product, comprising (a) contacting a nucleicacid array with reagents for nucleic acid expression to form a mixture,wherein the nucleic acid array comprises a first substrate and at least10 isolated coding nucleic acids physically confined at a discretelocation on a first substrate, and wherein each nucleic acid is capableof expressing its encoded product in situ at its discrete location onthe first substrate; (b) optionally, bringing the first substrate intothe proximity of a capture substrate; (c) incubating the mixture underconditions suitable for production of nucleic acid expression products;and (d) capturing and isolating the expression products on the firstsubstrate or, when present, the capture substrate. In one embodiment,the capture substrate comprises a second substrate that comprises aplurality of physically confined discrete locations that match thephysically confined discrete locations on the first substrate. Inanother embodiment, the methods comprise pre-coating the first substrateor the capture substrate, when present, with a first member of a bindingpair, wherein the expression products comprise a second member of thebinding pair, and wherein the incubating is done under conditionssuitable for binding of the first member and the second member of thebinding pair, resulting in capture of the expression product on thepre-coated substrate. In a further embodiment, the methods comprisepre-coating the first substrate or the capture substrate with a firstmember of a binding pair. In a further embodiment, the capture substrateis contacted to the first substrate to form a seal. In anotherembodiment, each discrete location comprises a well. In furtherembodiments, the nucleic acid expression comprises RNA expression and/orprotein expression. In another embodiment, the reagents comprise an invitro expression system. In a further embodiment, the methods comprisemodifying the polypeptide capture on the capture substrate. In a stillfurther embodiment, the methods comprise further stabilizing thecaptured polypeptides on the capture substrate to retain proteinfunctionality, such as by freezing the captured polypeptides on thecapture substrate.

DESCRIPTION OF THE FIGURES

FIG. 1 shows a side cut-through of an exemplary array substrate and anexemplary process for preparing and using the same.

FIG. 2 illustrates an exemplary method for filling and sealing nanowellson a substrate for product expression.

FIG. 3 shows the substrate of FIG. 2 having a sealed cover.

FIG. 4 illustrates an exemplary method for filling nanowells on asubstrate described herein.

FIG. 5 shows two separate results of a control experiment on glass, withfour drops of DNA & reagents dispensed in the center spot, proteinsproduced from the DNA using reticulocyte lysate and the proteins taggedwith fluorescently labeled antibodies.

FIG. 6 shows the same experiment as FIG. 5 using silicon nanowellsinstead of glass with 4 drops of DNA & reagents dispensed in the centerwell and reticulocyte lysate sealed within each nanowell.

FIG. 7 shows the same experiment as FIG. 6 with 8 drops of DNA &reagents dispensed in the center well.

FIG. 8 shows the same experiment as FIG. 6 with 16 drops of DNA &reagents dispensed in the center well.

FIG. 9 shows the same experiment as FIG. 6 with 32 drops of DNA &reagents dispensed in the center well.

FIG. 10 shows the same experiment as FIG. 9 with reticulocyte lysate notsealed within each nanowell.

FIG. 11 illustrates an exemplary process for expressing a product withina micro-capillary array.

FIG. 12 illustrates an exemplary method for detecting the presence offluorescent molecules within and on the surface of microcapillary tubes.

FIG. 13 is an image produced according to the method illustrated in FIG.12.

FIG. 14 is an image produced according to the method illustrated in FIG.12.

FIG. 15 illustrates a method for producing a protein array from a DNAarray by first printing a DNA array onto a surface, filling an array ofmicrocapillaries with reticulocyte lysate, aligning the array ofmicrocapillaries with the DNA array, bringing the array ofmicrocapillaries into contact with the DNA array, sealing the array ofmicrocapillaries and then incubating the assembly to produce proteinsfrom the DNA.

FIG. 16 illustrates an exemplary method of capture of an expressionproduct on a secondary (capture) surface using a substrate comprisingnanowells.

FIG. 17 illustrates an exemplary method of capture of an expressionproduct on a secondary (capture) surface using a substrate comprisingmicrocapillaries.

FIG. 18 illustrates an exemplary method for releasing a capturedexpression product from a substrate comprising microcapillaries.

FIG. 19 is a continuation of FIG. 18, showing methods for preparingarrays or capturing solutions of the released expression products.

FIG. 20 is a continuation of FIG. 18, showing exemplary diagnosticmethods using the released expression products.

FIG. 21 is a continuation of FIG. 18, showing other exemplary diagnosticmethods using the released expression products.

FIG. 22 is a continuation of FIG. 21, showing exemplary diagnosticmethods using the released expression products.

FIG. 23 illustrates an exemplary method for capturing an expressionproduct within the same nanowell as product expression.

FIG. 24 illustrates diffusion on glass slides for NAPPA at high arraydensities. (a) Schematic of NAPPA on glass, with array spacing less than400 microns. In-situ expressed proteins diffuse in the lysate mixtureand cross-bind at neighboring locations. As shown in the print layoutschematic to the left, for both (b) and (c), only the center spot wasprinted with DNA+printing-mix, while the surrounding spots were printedwith just printing-mix consisting of anti-GST capture antibodies (noDNA). (b) NAPPA on glass slides with feature period of 750 microns,showing no observable diffusion. (c) NAPPA on glass slides with featureperiod of 375 microns, showing visible diffusion.

FIG. 25 (a) Schematic of NAPPA in silicon nanowells; NAPPA samples werepiezo dispensed in the wells, which were then filled with lysate andpress-sealed with a compliant gasket film supported on a glass slab.Protein expression and subsequent capture by substrate-bound antibodyoccurred in confined nano-liter volumes, resulting in diffusion-freehigh density protein arrays (b) Method of fabrication of siliconnanowells; surface functionalization, printing and NAPPA expression (c)Cross-sectional SEM image of nanowells with 375 micron spacing (d)Engineering Arts au302 8-head piezo printer, dispensing on-the-fly intosilicon nanowells (e) Schematic of vacuum assisted filling mechanismdeveloped in-house to effectively fill silicon nanowells with IVTTlysate. Silicon nanowell slide is placed in the gasket cutout andsandwiched between the two frames. When the assembly is clamped a thinmicrofluidic chamber is formed over the slide, enabling filling andsealing proteins (f) Picture showing sealed nanowells filled withlysate.

FIG. 26 illustrates confined protein expression in sealed nanowells. (a)Schematic of 16 different genes printed into alternate wells, in a 7×7nanowell array (375 μm period) (b) Pico-green staining of printed DNA;to the right—3D profile of the signal showing intensity plotted againstx & y coordinates (c) Expression in unsealed nanowells detected using ananti-GST antibody. Expressed proteins diffuse locally andphysically-adsorb inside neighboring wells, displaying strong signal inall the wells (d) Expression in sealed nanowells detected using ananti-GST antibody. The empty wells in-between do not show any signal,implying no diffusion of protein from sealed wells. 3D profile ofprotein display to the right clearly shows diffusion-free signals insealed nanowells. (Refer to Supporting Information for cDNA printdetails).

FIG. 27 Demonstration of very high density protein arrays towards 24,000proteins on a single slide. 225 micron period nanowell arrays wereproduced in round-well and square-well geometries, by using differentsilicon wet-etch chemistries. In both cases, control printing-mix spots(no cDNA) were printed in a plus pattern around the central expressionspots. Neither the control printing-mix spots comprising antibodies northe surrounding empty spots show significant protein diffusion signal(a) Scanning electron microscope (SEM) images of 225 micron period roundsilicon wells in top and cross-sectional views; inset shows opticalmicroscope image (b) Schematic of print layout in 225 micron periodround nanowell array (c) Corresponding protein array display showinghigh intensity from center cDNA spots with no significant diffusionbackground (d) SEM and optical microscope images of square nanowellarrays in top and cross-sectional views (e) Schematic of print layout in225 micron period square nanowell array (f) Expressed proteins aredisplayed with strong signals (square shaped) from cDNA printednanowells, while printing-mix printed wells show signals at the sharpedges of the well (and empty wells show no discernible signal). Signalfrom square edges is thought to be due to preferential aggregation ofproteins and dye at the sharp edges of square wells.

DETAILED DESCRIPTION OF THE INVENTION

All references cited are herein incorporated by reference in theirentirety. Within this application, unless otherwise stated, thetechniques utilized may be found in any of several well-known referencessuch as: Molecular Cloning: A Laboratory Manual (Sambrook, et al., 1989,Cold Spring Harbor Laboratory Press), Gene Expression Technology(Methods in Enzymology, Vol. 185, edited by D. Goeddel, 1991. AcademicPress, San Diego, Calif.), “Guide to Protein Purification” in Methods inEnzymology (M. P. Deutshcer, ed., (1990) Academic Press, Inc.); PCRProtocols: A Guide to Methods and Applications (Innis, et al. 1990.Academic Press, San Diego, Calif.), Culture of Animal Cells: A Manual ofBasic Technique, 2^(nd) Ed. (R. I. Freshney. 1987. Liss, Inc. New York,N.Y.), Gene Transfer and Expression Protocols, pp. 109-128, ed. E. J.Murray, The Humana Press Inc., Clifton, N.J.), and the Ambion 1998Catalog (Ambion, Austin, Tex.).

All embodiments disclosed herein can be combined with other embodimentsunless the context clearly dictates otherwise.

Unless the context clearly requires otherwise, throughout thedescription and the claims, the words “comprise,” “comprising,” and thelike are to be construed in an inclusive sense as opposed to anexclusive or exhaustive sense; that is to say, in the sense of“including, but not limited to.” Words using the singular or pluralnumber also include the plural or singular number, respectively.Additionally, the words “herein,” “above,” and “below” and words ofsimilar import, when used in this application, shall refer to thisapplication as a whole and not to any particular portions of thisapplication. As used herein, the singular forms “a”, “an” and “the”include plural referents unless the context clearly dictates otherwise.“And” as used herein is interchangeably used with “or” unless expresslystated otherwise.

As used herein, the term “about” means within 5% of the recitedlimitation.

The description of embodiments of the disclosure is not intended to beexhaustive or to limit the disclosure to the precise form disclosed.While specific embodiments of, and examples for, the disclosure aredescribed herein for illustrative purposes, various equivalentmodifications are possible within the scope of the disclosure, as thoseskilled in the relevant art will recognize. For example, while methodsteps or functions are presented in a given order, alternativeembodiments may perform functions in a different order, or functions maybe performed substantially concurrently. The teachings of the disclosureprovided herein can be applied to other procedures or methods asappropriate. The various embodiments described herein can be combined toprovide further embodiments.

In one aspect, the disclosure provides biomolecule arrays, comprising(a) a first substrate; and (b) biomolecules comprising at least 10isolated coding nucleic acids and/or at least 10 isolated polypeptides,wherein each nucleic acid and/or polypeptide is physically confined at adiscrete location on the first substrate, and wherein each nucleic acidis capable of expressing its encoded product in situ at its discretelocation on the substrate, and/or wherein each polypeptide is capable ofa characteristic activity in situ at its discrete location on thesubstrate; wherein the discrete locations are separated from each otheron the first substrate by a center to center spacing of between about 20nm and about 1 mm.

The arrays of the invention can be used, for example, in high throughputgenomics and proteomics for specific uses including, but not limitedmolecular diagnostics for early detection, diagnosis, treatment,prognosis, monitoring clinical response, and protein crystallography.

Biomolecules of the present arrays can be a nucleic acid or apolypeptide that is capable of producing an expression product whenincubated with appropriate reagents (enzymes, buffers, salts,nucleotides, amino acids, ribosomes, etc.), or of being tested for aspecific activity on the substrate.

When the biomolecule is a polypeptide, such polypeptides may comprise orconsist of full length proteins, protein fragments, and naturallyoccurring and synthetic peptides. The polypeptides may includenon-naturally occurring amino acids and other modifications as desiredfor a given purpose.

When the biomolecule is a nucleic acid, the nucleic acid can be RNA orDNA. (e.g., a single-stranded DNA, or a double stranded DNA). In apreferred embodiment, the nucleic acid includes a plasmid or viral DNAor a fragment thereof; an amplification product (e.g., a productgenerated by RCA, PCR, NASBA); or a synthetic DNA. The nucleic acid mayfurther include one or more of: a transcription promoter; atranscription regulatory sequence; a untranslated leader sequence; asequence encoding a cleavage site; a recombination site; a 3′untranslated sequence; a transcriptional terminator; a sequence encodingan epitope tag; and an internal ribosome entry site. In anotherembodiment, the nucleic acid also includes a sequence encoding areporter protein, e.g., a protein whose abundance can be quantitated andcan provide an indication of the quantity of expression product. Thereporter protein can be attached to the nucleic acid expression product,e.g., covalently attached, e.g., attached as a translational fusion. Thereporter protein can be an enzyme, e.g., β-galactosidase,chloramphenicol acetyl transferase, β-glucuronidase, and so forth. Thereporter protein can produce or modulate light, e.g., a fluorescentprotein (e.g., green fluorescent protein, variants thereof, redfluorescent protein, variants thereof, and the like), and luciferase.The transcription promoter can be a prokaryotic promoter, a eukaryoticpromoter, or a viral promoter. The regulatory components, e.g., thetranscription promoter, can vary among nucleic acids at differentaddresses of the plurality. For example, different promoters can be usedto vary the amount of polypeptide produced at different addresses.

The biomolecules may be bound to the substrate, or may be unbound.Methods for binding biomolecules to substrates are well known in theart, as described below. The biomolecules at each discrete position canall be the same, or can vary from one position to another, as desiredfor any given purpose. The expression products may be the same at eachlocation, may differ at each location, or any other configuration, asdesirable for a given purpose.

As used herein, the term “substrate” refers to any type of solidsupport, such as the silicon-containing substrates described below, orany of the following substrates on which the biomolecules can bearrayed. Examples of such substrates include, but are not limited to,microarrays, beads, columns, optical fibers, wipes, nitrocellulose,nylon, glass, quartz, diazotized membranes (paper or nylon), silicones,polyformaldehyde, cellulose, cellulose acetate, paper, ceramics, metals,metalloids, semiconductive materials, coated beads, magnetic particles;plastics such as polyethylene, polypropylene, and polystyrene; andgel-forming materials, such as proteins (e.g., gelatins),lipopolysaccharides, silicates, agarose, polyacrylamides,methylmethracrylate polymers; sol gels; porous polymer hydrogels;nanostructured surfaces; nanotubes (such as carbon nanotubes,self-assembling-monolayers of functionalized molecules and nanoparticles(such as gold nanoparticles or quantum dots).

In other embodiments, the first substrate may be a thermoplastic moldedsubstrate via microtransfer molding or hot embossing from a suitablemold. The mold can be a patterned PDMS, silicon, or metal (e.g., Ni)mold prepared by methods familiar to those skilled in the art.

In one exemplary embodiment, the substrate comprises a substratesuitable for use in a “dipstick” device, such as one or more of thesubstrates disclosed above. When bound to a substrate, the biomoleculecan be directly linked to the support, or attached to the surface via alinker. Thus, the substrate and/or the biomolecules can be derivatizedusing methods known in the art to facilitate binding of the biomoleculesto the support. Other molecules, such as reference or control molecules,can be optionally immobilized on the surface as well. Methods forimmobilizing various types of molecules on a variety of surfaces arewell known to those of skill in the art. A wide variety of materials canbe used for the functionalized solid support surface including, but notlimited to, glass, gold or silicon for example.

The biomolecule is physically confined at a discrete location, such thatthe biomolecule is separated from biomolecules at other discretelocations by any suitable type of barrier. In various non-limitingembodiments, the discrete location can be a well, a tube, a patterned(chemical or mechanical) region of the substrate, a pillar (in relief),or any three-dimensional feature(s) that inhibit lateral diffusionbetween adjacent locations.

In one embodiment, the arrays and methods disclosed herein providedramatic improvements of protein microarrays; particularly to reducemanufacturing costs, improve quality and increase the density of NucleicAcid Programmable Arrays (NAPPA). NAPPA is a means of in situ expressionand capture of thousands of different proteins in a microarray format.In this method, DNA molecules corresponding to the proteins of interestare printed on the microarray substrate and then transcribed/translatedin situ at the time of assay. The DNA molecules are configured to appenda common epitope tag to all of the proteins on the N- or C-termini sothat they can be captured by a high-affinity capture reagent that isimmobilized along with the DNA and bovine serum albumen (BSA) and BS3cross-linker. In vitro transcription and translation (IVTT)-coupledreagents, such as rabbit reticulocyte lysate, are used to produce theprotein. The expressed protein is captured on the array through the highaffinity reagent that recognizes the epitope tag. NAPPA microarrays areused by researchers to concurrently study the interactions of thousandsof different proteins on the microarray surface with anotherbiomolecule, drug candidate or serum sample.

Physical confinement of the discrete locations prevents diffusionduring, for example, in vitro protein expression of NAPPA. In certainembodiments, each of the physically confined discrete locations cancomprise a well. As used herein, a well is a fluid receptacle that isopen at one end and closed at the other end. The wells can be of anydesired shape, including but not limited to circular, rectangular,square, polygonal, or arbitrarily shaped. Wells can be made by anysuitable technique, including but not limited to: photolithographyand/or isotropic or anisotropic etch in silicon wafers; forming asilicon-dioxide layer on top of the silicon wafer for compatibility withNAPPA chemistry that has been developed for glass (silicon-dioxide)surfaces; forming the nanowells by micro/Nano-imprinting of PDMS or byphotolithography of SUB; etching of glass or bonding a perforatedmembrane to a solid surface. In one embodiment, the substrates compriseone or more further features to improve sealing of wells duringbiochemical processing, when stored or in use. Sealing preventsmolecules from diffusing from one well to the next during a biochemicalprocesses, and is especially useful for high-density arrays with smallwell-to-well spacing. Such features include, but are not limited to, amating substrate that serves to seal each well; a lip around each well(where the lip comprises the same or different material as the substrateis made of), a silicone-rubber gasket around each well, and a matingsubstrate that forms a seal around each well of the substrate. Forexample, the mating substrate may have a compliant material to form atight seal between discrete locations when it is mated with thesubstrate.

In certain embodiments, each well has a diameter of between about 14 nmand about 0.75 mm. In various embodiments, the well diameters arebetween 20 nm and 500 μm; 50 nm and 500 μm; 100 nm and 500 μm; 250 nmand 500 μm; 500 nm and 500 μm; 1 μm and 500 μm; 10 μm and 500 μm; 100 μmand 500 μm; 150 μm and 500 μm; 20 nm and 300 μm; 50 nm and 300 μm; 100nm and 300 μm; 250 nm and 300 μm; 500 nm and 300 μm; 1 μm and 300 μm; 10μm and 300 μm; 100 μm and 300 μm; 150 μm and 300 μm; 20 nm and 250 μm;50 nm and 250 μm; 100 nm and 250 μm; 250 nm and 250 μm; 500 nm and 250μm; 1 μm and 250 μm; 10 μm and 250 μm; 100 μm and 250 μm; and 150 μm and250 μm.

The wells can be present on the first substrate at a density of betweenabout 250 billion wells per square centimeter and about 100 well persquare centimeter. In various embodiments, the wells are present on thefirst substrate at a density of between about 250 billion wells persquare centimeter and about 500 wells per square centimeter; about 250billion wells per square centimeter and about 1000 wells per squarecentimeter; about 250 billion wells per square centimeter and about10,000 wells per square centimeter; about 100 billion wells per squarecentimeter and about 100 wells per square centimeter; about 100 billionwells per square centimeter and about 500 wells per square centimeter;about 100 billion wells per square centimeter and about 1000 wells persquare centimeter; about 100 billion wells per square centimeter andabout 10,000 wells per square centimeter; about 10 billion wells persquare centimeter and about 100 wells per square centimeter; about 10billion wells per square centimeter and about 500 wells per squarecentimeter; about 10 billion wells per square centimeter and about 1000wells per square centimeter; about 10 billion wells per squarecentimeter and about 10.000 wells per square centimeter; about 1 billionwells per square centimeter and about 100 wells per square centimeter;about 1 billion wells per square centimeter and about 500 wells persquare centimeter; about 1 billion wells per square centimeter and about1000 wells per square centimeter; about 1 billion wells per squarecentimeter and about 10,000 wells per square centimeter; about 100million wells per square centimeter and about 100 wells per squarecentimeter; about 100 million wells per square centimeter and about 500wells per square centimeter; about 100 million wells per squarecentimeter and about 1000 wells per square centimeter; about 100 millionwells per square centimeter and about 10,000 wells per squarecentimeter; about 10 million wells per square centimeter and about 100wells per square centimeter; about 10 million wells per squarecentimeter and about 500 wells per square centimeter; about 10 millionwells per square centimeter and about 1000 wells per square centimeter;about 10 million wells per square centimeter and about 10.000 wells persquare centimeter; about 1 million wells per square centimeter and about100 wells per square centimeter; about 1 million wells per squarecentimeter and about 500 wells per square centimeter; about 1 millionwells per square centimeter and about 1000 wells per square centimeter;about 1 million wells per square centimeter and about 10,000 wells persquare centimeter; about 100,000 wells per square centimeter and about100 wells per square centimeter; about 100,000 wells per squarecentimeter and about 500 wells per square centimeter; about 100,000wells per square centimeter and about 1000 wells per square centimeter;about 100,000 wells per square centimeter and about 10,000 wells persquare centimeter; about 75,000 wells per square centimeter and about100 wells per square centimeter; about 75,000 wells per squarecentimeter and about 500 wells per square centimeter; about 75,000 wellsper square centimeter and about 1000 wells per square centimeter; about75,000 wells per square centimeter and about 10,000 wells per squarecentimeter; about 50,000 wells per square centimeter and about 100 wellsper square centimeter; about 50,000 wells per square centimeter andabout 500 wells per square centimeter; about 50,000 wells per squarecentimeter and about 1000 wells per square centimeter; and about 50,000wells per square centimeter and about 10,000 wells per squarecentimeter.

In various embodiments, the wells have a depth of between about 10 μmand about 150 μm; about 10 μm and about 125 μm; about 10 μm and about100 μm; about 10 μm and about 90 μm; about 10 μm and about 80 μm; about10 μm and about 75 μm; about 10 μm and about 70 μm; about 10 μm andabout 60 μm; about 10 μm and about 50 μm; 25 μm and about 100 μm; about25 μm and about 150 μm; about 25 μm and about 125 μm; about 25 μm andabout 100 μm; about 25 μm and about 90 μm; about 25 μm and about 80 μm;about 25 μm and about 75 μm; about 25 μm and about 70 μm; about 25 μmand about 60 μm; about 25 μm and about 50 μm; about 50 μm and about 150μm; about 50 μm and about 125 μm; about 50 μm and about 100 um; about 50μm and about 90 μm; and about 50 μm and about 75 μm.

In various embodiments, the wells have a period (i.e.: spacing) on thearray of between about 100 μm and about 400 μm; about 100 μm and about375 μm; about 100 μm and about 350 μm; about 100 μm and about 325 μm;about 100 μm and about 300 μm; about 100 μm and about 275 μm; about 100μm and about 250 μm; about 100 μm and about 225 μm; about 100 μm andabout 200 μm; about 100 μm and about 185 μm; about 100 μm and about 175μm; about 100 μm and about 150 μm; 125 μm and about 400 μm; about 125 μmand about 375 μm; about 125 μm and about 350 μm; about 125 μm and about325 μm; about 125 μm and about 300 μm; about 125 μm and about 275 μm;about 125 μm and about 250 μm; about 125 μm and about 225 μm; about 125μm and about 200 μm; about 125 μm and about 185 μm; about 125 μm andabout 175 μm; about 125 μm and about 150 μm; 150 μm and about 400 μm;about 150 μm and about 375 μm; about 150 μm and about 350 μm; about 150μm and about 325 μm; about 150 μm and about 300 μm; about 150 μm andabout 275 μm; about 150 μm and about 250 μm; about 150 μm and about 225μm; about 150 μm and about 200 μm; about 150 μm and about 185 μm; about150 μm and about 175 μm; 175 μm and about 400 μm; about 175 μm and about375 μm; about 175 μm and about 350 μm; about 175 μm and about 325 μm;about 175 μm and about 300 μm; about 175 μm and about 275 μm; about 175μm and about 250 μm; about 175 μm and about 225 μm; about 175 μm andabout 200 μm; about 175 μm and about 185 μm; about 185 μm and about 400μm; about 185 μm and about 375 μm; about 185 μm and about 350 μm; about185 μm and about 325 μm; about 185 μm and about 300 μm; about 185 μm andabout 275 μm; about 185 μm and about 250 μm; about 185 μm and about 225μm; and about 185 μm and about 200 μm.

In another embodiment, where well spacing (in mm) is “Sp”, density is“Dn”, diameter is “Dm”, and depth is “Dp”.

(a) the well density (in spots/mm̂2) is 1/Sp̂2<=Dn<=1/(Sp*(0.75)^(0.5))²;

(b) the well diameter (in mm) is 0.1*Sp<=Dm<=0.95*Sp; and/or

(c) the well depth is (in mm) is 0.1*Dm<=Dp<=3*Dm; and

In other embodiments, each physically confined discrete locationcomprises a tube (FIG. 11). As used herein, a tube is a fluid receptaclethat is open at both ends. The “tube” may be one or more (i.e.: 2, 3, 4,5, 6, 7, 8, 9, 10, or more) adjacent tubes in a single location. In onepreferred embodiment, a plurality of tubes in a discrete location isbundled together. In another embodiment, a plurality of tubes is fusedat one end with the other ends remaining separate. As a result, eachtube will, in use, receive the same fluid sample. The tubes can be ofany desired shape, including but not limited to circular, rectangular,square, polygonal or arbitrarily shaped.

Tubes can be made by any suitable technique, including but not limitedto: bundling glass capillaries together, fusing and drawing them out andthen slicing and polishing the result into thin sheets of fusednanotubes; photolithography and/or isotropic or anisotropic etch insilicon wafers; forming a silicon-dioxide layer on the surfaces of thenanotubes for compatibility with NAPPA chemistry that has been developedfor glass (silicon-dioxide) surfaces; forming the nanotubes bynano-imprinting of PDMS or by photolithography of SU8 or etching ofglass.

In certain embodiments, each tube can have an inner diameter of betweenabout 14 nm and about 0.75 mm. The tubes may be present on the firstsubstrate at a density of between about 250 billion tubes per squarecentimeter and about 1 tube per square centimeter. In another embodimentthe tubes are present on the first substrate at a density of betweenabout 250 billion tubes per square centimeter and about 10 tubes persquare centimeter. In another embodiment the wells are present on thefirst substrate at a density of between about 250 billion tubes persquare centimeter and about 100 tubes per square centimeter. Allembodiments of well diameter, period, and spacing on the array areequally applicable to tube inner diameter, period, and spacing. Tubedepth can be any suitable depth based on length of capillary tubes used.In one embodiment, tube length is between 10 nm and 10 mm. In variousfurther embodiments, the tube length is between 10 nm and 5 mm; 10 nmand 1 mm; 10 nm and 100 μm; 10 nm and 50 μm; 10 nm and 10 μm; 10 nm and1 μm; 10 nm and 100 nm; 25 nm and 10 mm; 25 nm and 5 mm; 25 nm and 1 mm;25 nm and 100 μm; 25 nm and 50 μm; 25 nm and 10 μm; 25 nm and 1 μm; 25nm and 100 nm; 50 nm and 10 mm; 50 nm and 5 mm; 50 nm and 1 mm; 50 nmand 100 μm; 50 nm and 50 μm; 50 nm and 10 μm; 50 nm and 1 μm; 25 nm and100 nm; 100 nm and 10 mm; 100 nm and 5 mm; 100 nm and 1 mm; 100 nm and100 μm; 100 nm and 50 μm; 100 nm and 10 μm; 100 nm and 1 μm; 500 nm and10 mm; 500 nm and 5 mm; 500 nm and 1 mm; 500 nm and 100 μm; 500 nm and50 μm; 500 nm and 10 μm; 500 nm and 1 μm; 1 μm and 10 mm; 1 μm and 5 mm;1 μm and 1 mm; 1 μm and 100 μm; 1 μm and 50 μm; 1 μm and 10 μm; 10 μmand 10 mm; 10 μm and 5 mm; 10 μm and 1 mm; 10 μm and 100 μm; 10 μm and50 μm; 100 μm and 10 mm; 100 μm and 5 mm; and 100 μm and 1 mm.

Each of the discrete locations may be additionally functionalized. Incertain embodiments, the surface is functionalized to be hydrophilic, asdescribed below. Such hydrophilic surfaces can promote wetting andspreading of reagents. In certain embodiments, the surface isfunctionalized to be hydrophobic, as described below. Such surfacefunctionalization may be within each discrete location or between thediscrete locations; in the latter case, the surface functionalizationmay serve to define the discrete locations. In one embodiment when thesubstrate comprises silicon, the Si substrates (such as substrates whereeach of the physically confined discrete locations comprises a well) maybe functionalized by coating with oxide, to reduce quenching offluorescence by Si. In this embodiment, any suitable thickness of oxidecan be coated on the substrate, such as between about 10 nm and 500 nmin thickness, preferably between about 50 nm and 250 nm in thickness, orabout 100 nm in thickness.

Each discrete location can further comprise reagents for expressing theencoded nucleic acid product and/or for testing polypeptide activity.Any suitable reagents for a given purpose can be used. Those of skill inthe art can determine appropriate reagents for a given use, based on theteachings herein combined with the level of skill in the art. In onenon-limiting example, where the biomolecule comprises a DNA molecule andthe desired expression product is a polypeptide, the reagents maycomprise a reticulocyte lysate.

For example, the reagents may comprise reagents for expressing theencoded nucleic acid product and/or for testing polypeptide activity andwhere those reagents are added to the array separately from the nucleicacids or polypeptides. The reagents can either by added prior to addingthe nucleic acids or polypeptides, or they can be added after thenucleic acids or polypeptides. For NAPPA for example, the reagentsconsist of a mixture of capture antibodies, BSA and BS3. This mixturecan be combined with the nucleic acids prior to printing them onto thearray surface or they can be printed separately. Furthermore, thenucleic acids can be printed onto the array surface with a suitablechemistry to bind them to the array surface and then the mixture can beflooded over the whole array surface. In particular embodiments, thereagent can comprise a reticulocyte lysate. The reticulocyte lysate canbe a solution (for example, added by an end user), or may be placed atthe discrete locations and frozen (for example, by a manufacturer), suchthat it can be stored, shipped, etc. Upon expression, the end productsmay be proteins that crystalize inside each physically confined discretelocation.

In certain embodiments, the biomolecules comprise at least 10 isolatedcoding nucleic acids. As will be clear to those of skill in the art,more than 10 isolated coding nucleic acids and/isolated polypeptides canbe arrayed on the substrate; in various embodiments, 50, 100, 500, 1000,2500, 5000, 10,000, 25,000, 50,000, 100,000, or more isolated codingnucleic acids and/isolated polypeptides can be arrayed on the substrate.In other embodiments, the biomolecules comprise at least 100 isolatedcoding nucleic acids; or at least 1000 isolated coding nucleic acids; orat least 10 isolated polypeptides; or at least 100 isolatedpolypeptides; or at least 1000 isolated polypeptides. In any of thepreceding embodiments, nucleic acids and/or polypeptides can be bound tothe substrate.

The arrays may further comprise either (i) a capture substrate adaptedto mate with the first substrate wherein the capture substrate isfunctionalized to capture and isolate the expression product; or (ii)the discrete locations are further functionalized to capture and isolatethe expression product. As used herein, “mate” means to form a seal,such that each of the discrete locations is completely separated fromeach other. However, a complete seal is not necessary, proximity, on theorder of micrometers, may be good enough in some cases. The capturesubstrate can be flat or it can have physical features that mate withthose on the first substrate. In certain embodiments, the capturesubstrate forms a complete seal with the first substrate. The capturesubstrate and/or the first substrate can have a compliant material toform a tight seal between discrete locations when the two are matedtogether.

In another aspect, the disclosure provides an array comprising asilicon-containing substrate, having a plurality of nanowells atdiscrete locations formed in a surface of the substrate wherein thediscrete locations are separated from each other on thesilicon-containing substrate by a center to center spacing of betweenabout 20 nm and about 1 mm; and biomolecules capable of capturinganother molecule located at each discrete location. In certainembodiments, the discrete locations are separated from each other on thefirst substrate by a center to center spacing of between about 20 nm andabout 100 μm. All embodiments of well diameter, period, depth, andspacing on the array provided above are equally applicable in thisaspect of the invention.

In one embodiment, the arrays comprise one or more further features toimprove sealing of wells when stored or in use. Such features include,but are not limited to, a lip around each well (where the lip comprisesthe same or different material as the substrate is made of), asilicone-rubber gasket around each well, and a mating substrate thatforms a seal around each well of the substrate. For example, the matingsubstrate may have a compliant material to form a tight seal betweendiscrete locations when it is mated with the substrate.

Examples of biomolecules which may be located in the nanowells at eachof the discrete locations include, but are not limited to, nucleicacids, antigen, antibodies, and the like, as discussed above. When thebiomolecule is a polypeptide, such polypeptides may comprise or consistof full length proteins, protein fragments, and naturally occurring andsynthetic peptides. The polypeptides may include non-naturally occurringamino acids and other modifications as desired for a given purpose.

When the biomolecule is a nucleic acid, the nucleic acid can be RNA orDNA. (e.g., a single-stranded DNA, or a double stranded DNA). In apreferred embodiment, the nucleic acid includes a plasmid or viral DNAor a fragment thereof; an amplification product (e.g., a productgenerated by RCA, PCR, NASBA); or a synthetic DNA. The nucleic acid mayfurther include one or more of: a transcription promoter; atranscription regulatory sequence; a untranslated leader sequence; asequence encoding a cleavage site; a recombination site; a 3′untranslated sequence; a transcriptional terminator; a sequence encodingan epitope tag; and an internal ribosome entry site. In anotherembodiment, the nucleic acid also includes a sequence encoding areporter protein, e.g., a protein whose abundance can be quantitated andcan provide an indication of the quantity of expression product. Thereporter protein can be attached to the nucleic acid expression product,e.g., covalently attached, e.g., attached as a translational fusion. Thereporter protein can be an enzyme, e.g., β-galactosidase,chloramphenicol acetyl transferase, β-glucuronidase, and so forth. Thereporter protein can produce or modulate light, e.g., a fluorescentprotein (e.g., green fluorescent protein, variants thereof, redfluorescent protein, variants thereof, and the like), and luciferase.The transcription promoter can be a prokaryotic promoter, a eukaryoticpromoter, or a viral promoter. The regulatory components, e.g., thetranscription promoter, can vary among nucleic acids at differentaddresses of the plurality. For example, different promoters can be usedto vary the amount of polypeptide produced at different addresses.

The biomolecules may be confined at the nanowells according to methodsfamiliar to those skilled in the art; for example, any of the precedingcan be attached to the surface of the nanowells on thesilicon-containing substrate through a divalent linking group to afunctional group capable of binding to or associating with the surfaceof the substrate, as discussed below.

Examples of molecules that the biomolecules may capture include, but arenot limited to, nucleic acid expression products when incubated withappropriate reagents (enzymes, buffers, salts, nucleotides, amino acids,ribosomes, etc.). In other embodiments, the biomolecules which maycapture and isolate the expression product include, but are not limitedto an antigen, inhibitor (e.g., an irreversible inhibitor), or anantibody for the expression product. Such surface functionalizations maybe introduced by methods familiar to those skilled in the art.

In certain embodiments, the silicon-containing (Si) substrate is asilica or silicon substrate. For example, the substrate may comprise aglass or a silicon wafer (each having a shape suitable for its intendedpurpose). Such substrates may be chemically patterned (e.g.,microcontact printing) or etched (e.g., standard masking and etchingmethods for silicon) according to methods known to those skilled in theart to provide a plurality of discrete locations on a surface thereof.For example, see e.g., Xia and Whitesides, Ann. Rev. Mater. Sci. 1998,28, 153, which is hereby incorporated by reference in its entirety.

In one embodiment, the Si nanowells are coated with oxide, to reducequenching of fluorescence by Si. In this embodiment, any suitablethickness of oxide can be coated on the substrate, such as between about10 nm and 500 nm in thickness, preferably between about 50 nm and 250 nmin thickness, or about 100 nm in thickness.

Suitable linking groups include, but are not limited to a group of theformula, —(C₀-C₁₀ alkyl-Q)₀₋₁-C₀-C₁₀ alkyl-, wherein Q is a bond, aryl,heteroaryl, C₃-C₈ cycloalkyl, or heterocyclyl; and no more than onemethylene in each alkyl group is optionally and independently replacedby —O—, —S—, —N(R⁰⁰)—, —C(H)═C(H)—, —C≡C—, —C(O)—, —S(O)—, —S(O)₂—,—P(O)(OH)—, —OP(O)(OH)—, —P(O)(OH)O—, —N(R⁰⁰)P(O)(OH)—,—P(O)(OH)N(R⁰⁰)—, —OP(O)(OH)O—, —OP(O)(OH)N(R⁰⁰)—, —N(R⁰⁰)P(O)(OH)O—,—N(R⁰⁰)P(O)(OH)N(R⁰⁰)—, —C(O)O—, —C(O)N(R⁰⁰)—, —OC(O)—, —N(R⁰⁰)C(O)—,—S(O)O—, —OS(O)—, —S(O)N(R⁰⁰)—, —N(R⁰⁰)S(O)—, —S(O)₂O—, —OS(O)₂—,—S(O)₂N(R⁰⁰)—, —N(R⁰⁰) S(O)₂—, OC(O)O—, —OC(O)N(R⁰⁰)—, —N(R⁰⁰)C(O)O—,—N(R⁰⁰)C(O)N(R⁰⁰)—, —OS(O)O—, —OS(O)N(R⁰⁰)—, —N(R⁰⁰)S(O)O—,—N(R⁰⁰)S(O)N(R⁰⁰)—, —OS(O)₂O—, —OS(O)₂N(R⁰⁰)—, —N(R⁰⁰)S(O)₂O—, or—N(R⁰⁰)S(O)₂N(R⁰⁰)—, wherein each R⁰⁰ is independently hydrogen or C₁-C₆alkyl.

Suitable functional groups include, but are not limited to —NH₂ (amine),—COOH (carboxyl), siloxane (—Si(OR)₃, where each R is C₁-C₄ alkyl), —OH(hydroxyl), —SH (mercapto), —CONH₂ (amido), —P(O)(OH)₂ (phosphonicacid), —S(O)₂OH (sulfonate), —S(O)OH (sulfinate), —OS(O)₂OH (sulfate),and chemical groups including the same.

The divalent linker may also comprise a photocleavable group within thedivalent group. Such surface functionalization can allow for expressionproducts to be isolated on the surface by binding with the biomoleculecapable of capturing the expression products. After expression, thesubstrate may be washed by methods familiar to those in the art toremove leftover starting materials, reactants, and/or contaminants.Then, the washed substrate may be exposed to a suitable wavelength oflight for a period of time suitable to cleave the photocleavable linker(FIG. 18), thereby releasing the expression product to allow furthermanipulation of the expression product (e.g., isolation on a secondsubstrate as discussed below).

The divalent linker may also comprise a chemically cleavable groupwithin the divalent group. Such surface functionalization can allow forexpression products to be isolated on the surface by binding with thebiomolecule capable of capturing the expression products. Afterexpression, the substrate may be washed by methods familiar to those inthe art to remove leftover starting materials, reactants, and/orcontaminants. Then, the washed substrate may be exposed to a suitablereagent for a period of time suitable to cleave the chemically cleavablelinker, thereby releasing the expression product to allow furthermanipulation of the expression product (e.g., isolation on a secondsubstrate as discussed below).

In certain embodiments, the surface is functionalized to be hydrophilic.Examples of hydrophilic functionalizations include, but are not limitedto hydroxyalkyl, aminoalkyl, or carboxyalkyl-functionalized siloxanes(for silica surfaces; e.g., 3-aminopropyl trimethoxysilane,(N,N-Dimethylaminopropyl)trimethoxysilane, or[3-(2-aminoethylamino)propyl]trimethoxysilane) and hydroxyalkyl-,amino-alkyl-, or carboxyalkyl-functionalized thiols (for metal surfaces,such as Au, Ag, Cu, Ni, Zn, or Pt, and the like; (e.g.11-Mercaptoundecyl)tetra(ethylene glycol);11-mercaptoundecyl)-N,N,N-trimethylammonium bromide;11-Mercapto-1-undecanol; 11-mercaptoundecanoic acid;11-mercaptoundecylphosphoric acid). As used herein, “hydrophilic” meansthat the location has a water contact angle less than 40 degrees asmeasured by the sessile drop method known to those skilled in the art.Such hydrophilic surfaces can promote wetting and spreading of reagents.

Such functionalizations may include use of a photoprotectedhydroxyalkyl, aminoalkyl, and/or carboxyalkyl-functionalized siloxanewhich may be photopatterned according to methods known to those skilledin the art to locally generate hydrophilic surfaces at discretelocations on the substrate surface. Such functionalizations may alsoinclude use of a reactive surface functionalization, such as an epoxy orisocyanato group which may be reacted with a second molecule (e.g.,1,2-diaminoethane) to generate a locally hydrophilic surface (e.g.,(triethoxysilyl)propyl isocyanate or3-glycidoxypropyldimethylethoxysilane).

‘In certain embodiments, the surface of the silicon-containing substrateis functionalized to be hydrophobic. Examples of hydrophobicfunctionalizations include, but are not limited to alkyl-functionalizedand fluoroalkyl-functionalized siloxanes (for silica surfaces; e.g.,1H,1H,2H,2H-perfluorooctyltriethoxysilane and dodecyltriethoxysilane)and alkyl-functionalized thiols (for metal surfaces, such as Au, Ag, Pt,and the like (e.g., 1-Dodecanethiol). As used herein, “hydrophobic”means that the location has a water contact angle greater than 90degrees as measured by the sessile drop method known to those skilled inthe art.

Such functionalizations to capture and isolate the expression productcan be located on a second substrate, or can be located within the samediscrete location on the first substrate. For example, an individualwell (e.g., rectangular sized or large elliptical/circular) can betreated such that one portion of the well has a nucleic acid (e.g., DNA)printed, and another portion has a coating of an antibody to theexpression product. An expressed protein can bind to this antibody toisolate the pure protein. That is, a “capture substrate” can be aseparate substrate from the silicon-containing substrate, or may be aportion of the silicon containing substrate available for use as tocapture expression products. In one non-limiting embodiment the “capturesubstrate” comprises one or more discrete locations on the substrateadjacent to the discrete location at which expression occurs, and thelocations are physically confined by a well or a tube (bottom capture,tube-wall capture or side capture etc.).

In another aspect, the disclosure provides methods for in situ nucleicacid expression, comprising

-   -   (a) contacting each discrete location of the array as described        in any of the preceding aspects and embodiments thereof, with        reagents for nucleic acid expression to form a mixture; and    -   (b) incubating the mixture under conditions suitable for nucleic        acid expression.

In yet another aspect, the disclosure provides methods for expressingand capturing an expression product, comprising

-   -   (a) contacting a nucleic acid array with reagents for nucleic        acid expression to form a mixture, wherein the nucleic acid        array comprises a first substrate and at least 10 isolated        coding nucleic acids physically confined at a discrete location        on a first substrate, and wherein each nucleic acid is capable        of expressing its encoded product in situ at its discrete        location on the first substrate;    -   (b) optionally, the first substrate may be brought into the        proximity of a capture substrate;    -   (c) incubating the mixture under conditions suitable for        production of nucleic acid expression products; and    -   (d) capturing and isolating the expression products on the first        substrate or, when present, the capture substrate.

It is well within the level of those of skill in the art to determinethe most appropriate conditions for the contacting, incubating, andcapturing steps based on the teachings herein. In one non-limitingexample, conditions for NAPPA typically comprise incubating the DNA of1-2 hours at 30° C. to express proteins.

The expressed product may be captured on the same first substrate or thecapture substrate. For example, each of the discrete locations mayfurther comprise a biomolecule capable of binding to or associating withthe expressed product, as discussed herein, such that the expressionproduct is produced and captured at the discrete location. In anotherexample, the first substrate may be contacted with a capture substrate,where the capture substrate is coated with a biomolecule capable ofbonding to or associating with the expressed product; upon expression,the product can be captured on the capture substrate. Exemplary capturesubstrates and their use are provided in FIGS. 16-17. FIG. 16 (well) andFIG. 17 (capillary tubes) show embodiments in which capture antibodiesare coated on glass slides (and not in the DNA/reagent mixture in thewells) that act as the capture substrate; contacting this capturesubstrate with the array and carrying out protein expression results ina capture substrate that is a pure protein array and does not containthe stating DNA or reagents. The capture substrates may be made of anymaterial or comprise any other components suitable for a given use,including but not limited to gold and/or silver coated capturesubstrates (for example, for use in surface plasmon resonance (SPR)studies), capture substrates that comprise field effect nanowires (forexample, to produce substrates having nanowires coated with theexpressed proteins), and capture substrates comprising spin-coated probemolecules magnetic micro/nanoparticles coated with secondary antibodiesor chemical linkers.

Using the methods of the invention, expression products can be expressedmultiple times from the same array, enabling more than oneisolated-expression product capture per array. Herein, ‘isolated’ meansthat the DNA print location is separated from the capture location ofthe expression product and not contaminated by other biologicalmaterial. (e.g., in regular NAPPA both these locations are the same).

The contacting can be done under any conditions suitable for a givenpurpose. In one embodiment, the reagents can be flooded across alldiscrete locations. In another embodiment, the reagents can bediscretely delivered to some or all discrete locations, for example,using known microfluidic techniques. As will be understood by those ofskill in the art, the arrays may be generated and used immediately, orthe arrays may be generated and stored for later use. When arrays aregenerated and stored for later use, the reagents (such as reticulocytelysate) may be added at the time of use or the array/reagents may begenerated and stored frozen, such that at the time of use the lysate isunfrozen and incubated as appropriate. In a further embodiment, thearrays may be frozen after the incubating/protein expression and anydesired subsequent steps, for later use of the expressed proteins.

In various non-limiting embodiments of any of the preceding aspects andembodiments thereof, the methods may comprise one or more of thefollowing:

-   -   (a) Filling and sealing the discrete locations (such as        nanowells) during polypeptide expression to prevent cross        contamination between neighboring wells. For example, plasmid        DNA in the nanowells is exposed to reagents, such as        reticulocyte lysate, to express proteins from the DNA (e.g., use        pre-vacuumed PDMS wells (or another foamy substrate like        silicone rubber foam), where residual vacuum sucks lysate in; or        e.g., fill wells with water first, remove water other than        inside of wells, and then inject lysate to displace/mix water        with lysate).    -   (b) using a rigid cover with spacers between a cover (as used        herein, including but not limited to a capture substrate) and        substrate array surface, followed by removal of the spacers to        push down the cover-plate and seal the discrete locations;    -   (c) using a rigid cover-plate with elastic spacers between a        cover and the discrete locations, followed by pushing down on        the cover-plate to compress the elastic spacers to seal the        discrete locations;    -   (d) using a flexible cover and pushing down on a cover to deform        it and seal the discrete locations;    -   (e) forcing the reagents, such as reticulocyte lysate fluid        through a narrow gap between the substrate and a cover to spread        the fluid uniformly over the array surface;    -   (f) filling the discrete locations (such as nanowells or tubes)        with reagents, such as reticulocyte lysate using vacuum, syringe        and solenoid-valve. See, for example, FIG. 4. Assembling a        cover-plate, with two holes, over the substrate. Sealing the        cover-plate to the substrate around the edges. Leaving a gap        between the cover-plate and the substrate. Attaching a syringe        to a solenoid-valve with just enough reticulocyte lysate to fill        the discrete locations, the gap over the substrate and the        assorted valves, fittings and tubing. Attaching the other end of        the solenoid-valve to one of the holes in the cover-plate.        Applying a vacuum to the other hole in the cover-plate. Opening        the solenoid valve. Releasing the vacuum. This embodiment can be        varied by one or more of:        -   (1) replacing the solenoid-valve with a septum and piercing            the septum with a syringe needle attached to the syringe to            start the flow of reagents into the device;        -   (2) eliminating the solenoid-valve, holding back the flow of            reagents using a mechanical stopper on the syringe plunger            and then releasing the mechanical stopper to start the flow            of reagents into the device;        -   (3) eliminating the solenoid-valve, holding back the flow of            reagents using a syringe pump and then moving the syringe            pump forward to start the flow of reagents into the device;        -   (4) placing a flow restrictor in line with the            solenoid-valve to slow down the flow rate if necessary;        -   (5) adding mechanical damping to slow down the movement of            the syringe plunger if necessary;        -   (6) adjusting the gap between the substrate and the            cover-plate to obtain uniform filling of all of the discrete            locations; and        -   (7) attaching a single syringe of reticulocyte lysate to            multiple arrays to simultaneously fill more than one array            at a time.    -   (g) orienting the substrate vertically and submerging it, at a        controlled rate, into a reagent thereby displacing air from the        nanowells by the reagent;    -   (h) orienting the substrate vertically and submerging it, at a        controlled rate, into a reagent while vibrating the reagent to        further assist in displacing air from the nanowells by the        reagent;    -   (i) placing the substrate vertically into a vessel and filling        the vessel from the bottom at a controlled rate with a reagent        thereby displacing air from the nanowells by the reagent;    -   (j) placing the substrate vertically into a vessel and filling        the vessel from the bottom at a controlled rate with a reagent        while vibrating the reagent thereby further displacing air from        the nanowells by the reagent;    -   (k) filling the discrete locations with reagents, such as        reticulocyte lysate inside of a vacuum chamber. Assembling a        cover-plate, with one hole, over the nanowell array surface.        Sealing the cover-plate to the nanowell array surface around the        edges. Leaving a gap between the cover-plate and the nanowell        array surface. Placing a drop of reticulocyte lysate over the        hole and putting the assembly into a vacuum chamber. Appling a        vacuum to the vacuum chamber and waiting until all of the air        from the gap escapes through the small hole in the cover plate.        Removing the vacuum thus forcing the reticulocyte lysate into        the small hole and onto the nanowell array surface.    -   (l) Filling the discrete locations of the substrate with        reagents while the substrate is vibrating to release any air        bubbles entrapped within the discrete locations.    -   (m) Adding a lip around each discrete location (such as        nanowells) with a lip for improved sealing.    -   (n) Adding a thin film (which can optionally be transparent)        between a silicone rubber and the wells.    -   (o) Using a thin film and air pressure to seal the wells instead        of silicone rubber.        -   Regulate the temperature of the liquid for thermal cycling            of the reaction process.

In another embodiment, a microsieve membrane can be used to cover thearray. For example (relating to improved NAPPA), print NAPPA mixtures onthe substrate. Using precise tooling, align the pores of the membrane tothe NAPPA spots. Expose the NAPPA spots to reticulocyte lysate throughthe pores in the membrane to isolate protein expression withinindividual spots. Maintain an air-gap between the bottom of themicrosieve-membrane and the top of the flat microarray surface. Howeverallow the reticulocyte to bridge the gap. Make physical contact betweenthe bottom of the microsieve-membrane and the top of the microarraysurface. Use a highly perforated microsieve-membrane with very small,closely-packed pores so that multiple pores cover one NAPPA spot. Thisalleviates the need for precise alignment of the microsieve-membrane andthe microarray surface. Based on the teachings herein, it is within thelevel of skill in the art to determine appropriate reagents andincubation conditions to use for an intended use.

“Capture substrate” as used herein can be a separate substrate from thefirst substrate, or may be a portion of the first substrate availablefor use as to capture expression products. In one non-limitingembodiment the “capture substrate” comprises one or more discretelocations on the substrate side by side with the discrete location atwhich expression occurs, and the locations are physically confined by awell or a tube (bottom capture, tube-wall capture or side capture etc.).

In one embodiment, the capture substrate comprises a second substratethat comprises a plurality of physically confined discrete locationsthat match the physically confined discrete locations on the firstsubstrate. The capture substrate can be one or more further substrates,as appropriate for any intended use. Any arrangement of discretelocations on the second substrate can be used that is suitable for agiven expression product capture method. In one non-limiting embodiment,each discrete location on second substrate comprises pre-patternedlocations/array of devices or chemical patterns or material filmpatterns. In various non-limiting embodiments, gold nanodots can be usedto generate plasmonic sensors, nanowire arrays can be used to generatefield effect sensors, and meso-porous alumina/gold pads can be used togenerate electrochemical sensors.

In another non-limiting embodiment, each discrete location on the secondsubstrate comprises an array of nano-holes with lipid bi-layers, whereinlipid bi-layers capture expressed polypeptides to produce membranepolypeptides.

In a further non-limiting embodiment, multiplicities of second discretelocations are provided on different capture substrates. In onenon-limiting example of this embodiment, multiple capture substrates canbe used for each nucleic acid array (e.g., reusable)

In yet another non-limiting embodiment, the discrete locations comprisesurfaces of micro or nano particles introduced into the confined spaceson the capture substrate. In one example of this embodiment, gold ormagnetic micro/nano particles can be introduced into the discretelocations to create particles where surfaces are covered with individualpolypeptides after capture.

In various further embodiments, the capture substrate is applied/subjectto any one, or a combination of, a varying potential/voltage/current orapplication of a magnetic field or application of a temperature or amechanical force, as appropriate for an intended use. In one example,electrochemical oxidation/reduction can be used to induce cover captureon metal or dielectric substrates.

In another embodiment, the cover-capture surface can be nano-structuredto increase surface capture area and/or surface roughness, there-bybinding more expression product, for increased signal. In anotherembodiment, etched/frosted glass (chemical or physical etch) can be usedto provide a rough surface for coating with capture reagent.

In certain embodiments of any of the preceding methods, the firstsubstrate or the capture substrate can be precoated with a first memberof a binding pair, wherein the expression products comprise a secondmember of the binding pair, and wherein the incubating is done underconditions suitable for binding of the first member and the secondmember of the binding pair, resulting in capture of the expressionproduct on the precoated substrate.

Any suitable binding pairs can be used for a given purpose. In oneexample, the substrate is pre-coated with biotin, and the biomoleculeexpression product comprises a streptavidin tag. Once the sequence forthe streptavidin tag is expressed, it binds the expressed protein to thebiotin-coated substrate. As will be apparent to those of skill in theart, many such permutations are possible, all of which are contemplatedherein. For example another suitable binding pair comprises halotagprotein and halotag ligands. In another example an E-coil tag on theexpression product binds to a K-coil peptide immobilized on thesubstrate.

In other embodiments of any of the preceding methods, the firstsubstrate is precoated with a first member of a binding pair. In otherembodiments of any of the preceding methods, the capture substrate isprecoated with a first member of a binding pair.

The capture substrate can be contacted to the first substrate to form aseal. In this embodiment, a seal is made so that each of the discretelocations is completely separated from each other. In certainembodiments, each discrete location comprises a well. In certain otherembodiments, each discrete location comprises a tube. The tubes may beof any suitable type for a given purpose. In one embodiment, tubes canbe commercially obtained from, for example, Incom or other vendors, asnoted above.

In one embodiment, NAPPA mixtures are dispensed into the tubes in anarray format. For example, the inside of the tubes can be flooded withreticulocyte lysate to express polypeptides and capture them on theinside walls of the tubes. Optionally, both ends of the tubes can besealed during polypeptide expression and capture. For detection, thearray can be imaged by any suitable technique, including but not limitedto illuminating the array from one-end and detecting fluorescent signalat the other end taking advantage of the light-guide properties of thearrangement. In another embodiment, a user can optionally hold thelight-source at an angle to increase signal strength (FIG. 12).Exemplary methods for expressing a product within a tube array (FIG. 13)and for detecting the presence of fluorescent molecules within and onthe surface of the tubes (FIG. 14) are provided. cDNA was diluted withreagent mix and placed into the tubes. The tubes were then filled withreticulocyte lysate and expressed as usual in NAPPA. When the NAPPAprint mix is dilute enough the print mixture with cDNA is deposited onthe side of tubes. If the print mix is too concentrated, it may blockthe tubes, making it more difficult to introduce the lysate. cDNAcoating on the side of the tubes facilitates filling with lysate andexpression. In this case the final image shows a clear internal ring offluorescent signal, inside of the tubes corresponding to printedlocations.

In certain embodiments, nucleic acid expression comprises RNAexpression. In other embodiments, the nucleic acid expression comprisespolypeptide expression. Accordingly, the reagents may comprise an invitro expression system. Any suitable in-vitro expression system can beused, including: but not limited to reticulocyte lysates, insect celllysates and human cell lysates.

The method may further comprise modifying the polypeptide capture on thecapture substrate. Any suitable modification of the polypeptide can bemade as appropriate for an intended use. In one non-limiting embodiment,the bound/captured polypeptide is post-translationally modified usingthe same or a secondary reagent that may be present in the expressionmixture or added after the expression-capture. This embodiment may becarried out on the capture substrate only, or may include a thirdsubstrate. The method may further comprise stabilizing the capturedpolypeptides on the capture substrate to limit protein diffusion.Stabilizing may be, for example but not limited to, freezing thecaptured polypeptides on the capture substrate.

The captured proteins on the capture-reagent coated surface may be usedto carry out one or more process selected from the group consisting ofsurface plasmon resonance (SPR) detection, MALDI mass spectrometry, andpost-translational modification.

In another aspect, the invention provides methods for detectingbiomolecules on any of the arrays described in the preceding aspect andembodiments thereof, comprising, scanning the arrays at various depthsand combining the intensity reading at each pixel of the resultingscanned images. As used herein, ‘combining’ means calculating anysuitable mathematical norm of the pixel intensities, including but notlimited to the average or peak value, for the purpose of uniformlyincreasing the detection signal across discrete locations. Typicalmicroarray scanners used for fluorescent detection of biomolecules aredesigned to scan a flat surface and consequently have limited depth offield. However the discrete locations disclosed here may be threedimensional. Scanning these locations at various focal depths and thencombining the resulting images circumvents limitations due to thelimited depth of field of microarray scanners for this application.

One non-limiting embodiment of the arrays of the invention and theirpreparation and use is provided in FIG. 1, and has 50 μm depth wellsthat have 35° walls and 145 μm diameter, where the wells have a 225 μmperiod. Substrates containing such arrays can be obtained, for example,from etched silicon or etched glass. The wells can be functionalizedwith amino silane prior to printing of cDNA on the bottom of the wells(or alternatively the cover) and filled with reticulocyte lysate,followed by use of a cover to squeeze out excess reticulocyte lysate andseal the microwells (FIGS. 2-3). The arrays can then be incubated for0.5 to 2 hours to transcribe and translate the protein encoded by thecDNA.

FIGS. 5-10 show the results of experiments in which a controlled amountof DNA and reagents are dispensed either on glass or in wells, showingthe significant improvement in reducing diffusion using the arrays andmethods of the invention. FIG. 5 shows a control experiment on glass,with four drops of DNA & reagents dispensed in the center spot, proteinsproduced from the DNA using reticulocyte lysate and the proteins taggedwith fluorescently labeled antibodies; significant diffusion betweenspots is evident in the detected fluorescence pattern. FIG. 6 shows thesame experiment as FIG. 5 using sealed silicon nanowells with a periodof between 200-225 μm instead of glass, with a resulting significantreduction in diffusion of fluorescence from one well to another. FIGS.7-9 show similar results using increasing amounts of DNA and reagentsper well, while FIG. 10 shows that the cover seal helps to limitdiffusion between wells.

In one embodiment employing microcapillaries, FIG. 18 shows a method forreleasing a captured expression product from a substrate comprisingmicrocapillaries via cleavage of a cleavable linker (chemical orphoto-induced), or by competing with excess antibody or antigen. Theexpressed proteins are thus suspended in solution, producing an array ofproteins in solution phase, which can be stored in any suitable manner.For example, the array can be sealed with sealing/capture substrate oneither or both side of the array and frozen for storage or shipment(FIG. 19). When ready to be used, the user can transfer the proteinsonto the substrate just before use, or can use the arrays in any othersuitable manner. In other embodiments, the arrays can be sealed with acapture substrate (including but not limited to gold and/or silvercoated surfaces) suitable for use in surface plasmon resonance (SPR),allowing the resulting arrays on the capture substrate to be used inSPR-based detection/diagnostics or other suitable studies.Alternatively, the array can be sealed with a capture substrate thatcomprises field effect nanowires, where the resulting capture substratehas nanowires coated with the expressed proteins, for use in diagnosticor other suitable sensing procedures (FIG. 20). Other exemplifiedcapture substrates include those with spin-coated probe molecules orcapture substrates with magnetic micro/nanoparticles coated withsecondary antibodies or chemical linkers and applied to the capturesubstrate using spin coating or microfluidics. (FIGS. 21-22)

Those of skill in the art will understand that all of these exemplifiedembodiments can also be used with well-based embodiments of the arrays,or any other embodiment of the means for physical confinement.

FIG. 23 shows an embodiment for capturing an expression product withinthe same nanowell where expression occurred. In this embodiment, siliconnanowells are coated with ligands for a tag expressed as part of theprotein product to be expressed. Plasmid DNA encoding the taggedexpression products of interest is printed in the microwells via anysuitable technique, such as via a piezoelectric arrayer. Reticulocytelysate is then placed in the wells via any suitable technique, such asby flooding all of the wells or dispensing into individual wells using apiezoelectric arrayer, and the wells are sealed. The array is incubatedunder suitable conditions for protein expression, and expressed taggedproteins will be captured by ligands in the wells. The sealing means isremoved and the wells washed under conditions suitable to remove unboundmaterials. Bound proteins are contacted with any suitable reagent, suchas reagents/conditions suitable for citrullination of the boundproteins, which can then be detected by incubation under suitableconditions to bind anti-citrulline antibodies/fluorescently labeledsecondary antibodies.

EXAMPLES

In this study, we sought to determine whether in situ synthesis of NAPPAreactions suffered from diffusion-related cross-talk at higher arraydensities. We then sought to solve the problem of diffusion with aninnovative silicon nanowell platform that used the NAPPA protein arrayssystem as a test case. This platform enables confined biochemicalreactions in physically separated nanowells. The NAPPA method wasadapted to nanowell array substrates produced using silicon microfabrication technology, which enables high-throughput, high-fidelityfabrication of nanowell substrates. We have also simultaneouslydeveloped a precise and accurate high-throughput liquid dispensingsystem to align and dispense genes and reagents into individual wells.After in vitro expression of proteins in the nanowells with a sealedcover, we demonstrated successful protein display in wells withnegligible diffusion. Preliminary results also indicated functionalprotein that allows detection of known protein-protein interactions. Ourdevelopment represents a major step forward in the production offunctional human proteome protein arrays without diffusion of solublespecies from feature to feature.

Results NAPPA on Glass Slides

We tested the effect of reduced spacing of features using NAPPA.Diffusion of expressed proteins captured at neighboring locations becamesignificant as separation distances (center-to center) drop below 400microns on NAPPA. This is demonstrated in FIG. 24 where genes wereprinted on planar glass in two different array densities: a low densityarray with a 750 micron period (FIG. 24 b) and a high density array witha 375 micron period (FIG. 24 c). The features were printed in a patternsuch that the center feature, containing cDNA+printing-mix, wassurrounded by control features, where the control features containedonly capture antibody (no genes). This configuration is highly sensitivefor detection of cross-contamination because the control features do notproduce protein that could compete with diffused protein. As illustratedin the 3-D rendering (FIG. 24), there was significant diffusion toneighboring features at 375 micron spacing compared to minimal diffusionfor the 750 micron period array. The halo of signal around the centerspot seen in both images is probably due to protein diffusion followedby physisorption to amine coated glass surface, and the shift of halooff-center may be due to fluid drift.

NAPPA in Silicon Nanowells

To enable high density printing without diffusion, we replaced planarglass slides with slides comprising an array of nanowells on the siliconsubstrate and sealed the wells during protein expression (FIG. 25).Adapting the NAPPA method to the nanowell platform enables physicallyconfining protein expression and the ensuing antibody capture innanoliter volumes (volume of nanowells ≦5 nanoliter). Expressed proteinsare free to diffuse within the individual sealed wells until they arecaptured by the anti-GST antibodies in the wells. Semi-sphericalnanowell arrays, approximately 250 microns in diameter and 75 micronsdeep with a period of 375 microns, were fabricated on silicon wafers,diced into the shape of glass slides (1 inch×3 inch), and used assubstrates for protein display. Monolithic crystalline silicon waferswere chosen due to the established silicon processing techniques thatallow for well-controlled and inexpensive fabrication of nanowell arrayslides. Wells were etched by photo-patterning silicon-nitride mask layerdeposited on silicon, using HNA isotropic etch chemistry (see alsoMaterials and Methods). Nanowells etched in silicon were coated with 100nm of dry oxide grown at 1,000 C in an oxidation furnace. Semiconductingsilicon acts to quench surface fluorescence due to its semimetallicnature, hence requiring 100 nm thin layer of oxide dielectric layer.Additionally, thermally grown silicon dioxide serves as high qualityglass surface for subsequent aminopropyltriethoxy silane (APTES) coatingand appropriate NAPPA chemistry.

Non-Contact Piezoelectric Dispensing

Standard solid pin printing would not suffice for the precision that isrequired in printing expression mixtures into the nanowells. Thus, wedeveloped a new method using piezoelectric printing. NAPPA expressionmixtures were piezo-jet dispensed into APTES coated silicon nanowells(SiNW) using Engineering Arts' 8-tip au302 piezo printer, capable ofaligning and printing at the center of the nanowells at very high-speeds(FIG. 25 c). One of the key challenges of nanowell technology is precisealignment and dispensing of many “unique” printing solutions onto abatch of nanowell slides in a suitable time frame. Special dispensehardware and software were developed that utilized the 8 headnon-contact “on-the-fly” dispense technology resulting in a batchprocessing time of a few hours to fill 7,000 wells each slide, on abatch of up to 8 nanowell slides (details in methods section).

Vacuum Assisted SiNW Filling of Nanowells

After printing, NAPPA SiNW slides were first subjected to vacuuminfiltration by de-ionized water for 5 to 10 minutes followed by vacuuminfiltration by SuperBlock TBS (Thermo Scientific) solution for 5 to 10minutes and subsequently incubated at room temperature and atmosphericpressure on a rocking shaker for 30 to 60 minutes. The slides were thenrinsed thoroughly with de-ionized water and dried under a gentle streamof filtered compressed air. Any unbound or loosely bound material (DNA,anti-GST, BSA, BS3 crosslinker or trace DMSO) should wash away duringthese pre-hybridization blocking and washing steps; thereby minimizingthe chance for material to break loose during subsequent steps. Afterblocking, the SiNW slides were incubated with rabbit reticulocytelysate-(RRL) based in vitro transcription and translation (IVTT) systemfor protein expression and capture in situ. When this viscous lysate wasdirectly introduced onto a slide with an array of nanowells, itexhibited a tendency to flow over the nanowells entrapping air withoutfilling the wells (data not shown). This is an expected behavior due toliquid surface-tension where cohesive-forces tend to minimize the liquidsurface area. To address this problem, we developed a vacuum-assistedfilling procedure (FIG. 25 d,e), which works independently of: the sizeand shape of nanowells; the fluid properties of filling liquid; or theproperties of nanowell substrate.

In this procedure an enclosed air-tight micro-chamber is created overthe nanowell slide by sandwiching the SiNW slide between a gasket cutoutand two planar surfaces as shown in FIG. 25 d. An inflexible metal plateforms the bottom planar surface, while the top surface is made bysticking a thin film of flexible transparent silicone on thickinflexible glass slab held on a metal frame. Two 1.5 mm wide 100 micronthick adhesive-backed plastic strips (not shown in schematic) areapplied manually along the long edges of the SiNW slide. The assembly isclamped on all sides and pressed together to reduce the height(thickness) of air-tight microchamber to approximately 100 microns, withthe top surface compressing the surrounding gasket cutout and resting onthe side strips on SiNW slide.

Lysate was introduced into the syringe attached to the port (a 1 mmdiameter hole on top plate) as shown, and was held in-place inside thesyringe due to the airtight micro-chamber (FIG. 25 d). Air inside themicro-chamber and air dissolved in the lysate solution was removed byapplying a gradual vacuum (up to 28 inches Hg) for 2 minutes. Using athree way solenoid valve (adapters and solenoid not shown) the syringewas then instantly switched from vacuum to atmospheric pressure. Onceswitched, the pressure difference, i.e., atmospheric pressure acting onthe lysate solution against vacuum in the wells, drove the liquid intofilling all the nanowells effectively in less than two seconds. Thisin-house developed vacuum-assisted filling system ensured a goodpressure seal by virtue of the transparent flexible silicone filmsupported on glass slab (inset image of sealed silicon nanowells, FIG.25 e). The silicone film, under applied pressure, conforms around thenarrow top edges of wells, to seal the nanowells. The sealed assemblywas then incubated for protein expression and binding.

Minimal Protein Diffusion Between Nanowells Using SiNW

To test protein expression and capture in silicon nanowells and toassess the level of cross-talk between the nanowells, sixteen differentgenes were printed into every other nanowell, (schematic of printpattern in FIG. 26 a). Intervening wells were left empty, and signalsobserved in these intervening wells would indicate the level ofcross-contamination due to diffusion. Pico-green staining of printed DNAshowed the expected alternate fluorescent signals (FIG. 26 b),confirming precise “on-the-fly” dispensing by the piezo printer into thewells. When the nanowells were left un-sealed (without clamping) duringprotein expression, spillover signal was observed in intervening wells(FIG. 26 c). Whereas, display of expressed and captured proteins insealed nanowells is shown in FIG. 26 d. As seen from the image and its3D signal profile, there was no discernible diffusion of proteins fromexpression wells to neighboring empty wells.

High Density NAPPA Protein Array

After successfully demonstrating precise dispensing and confinedexpression with a small number of genes, we produced SiNW slides with anarray of 8,000 nanowells (SiNW-8K chip, 375 um feature distances). Thesewere used to confirm diffusion-free expression across the footprint of afull size microscopic slide for a large number of genes in sealednanowells (not shown). Two-hundred eighty-seven (287) randomly selectedgenes, 192 from Vibrio cholerae and 96 from human, were printed inblocks of 6 rows×48 columns, which was repeat printed 24 times. TP53,FOS and JUN proteins were interspersed in the block pattern, with p53protein repeat printed twice in each block. The DNASU logo was printedby pooling 8 different genes into a single composition (no p53). Theprint pattern also included empty nanowells around the above array, andsurrounding the logo at the bottom, as negative controls. Consistent andprecise dispensing across the whole array was shown by the picogreenstaining of printed DNA (not shown). Overall, the array showedconsistently high protein expression as detected by anti-GST staining.

Diffusion-Free High Density Protein Arrays

The principle aim of this work—to solve the issue of diffusion in veryhigh density arrays—has been successfully addressed. Almost all emptyspots around the print block and empties surrounding the DNASU logoshowed no significant signal above background.

To further confirm diffusion-free protein display, we used a moresensitive test to assess diffusion by probing the high density NAPPA inSiNW with antigen specific antibodies against TP53 protein to determineif its signal was observed in neighboring wells (not shown). The ratioof average signal from neighbor spots to average signal from cognate p53spots was calculated to be just 1.34%. This confirms that very highdensity in-situ protein arrays can be successfully produced usingnanowells to arrest protein diffusion and cross-binding. Analyzing thep53 signals, the coefficient of variation (CV) between the 48 repeatspots is calculated to be 12.84%.

Discounting the one outlier low-signal p53 spot on bottom right side,the CV was calculated to be 8.5%.

Functional Studies on Nanowell Protein Arrays

To investigate the functionality of the proteins produced in nanowells,we examined protein-protein interactions using the well-establishedFOS-JUN interaction (16) as a surrogate assay for proper folding andfunctionality of proteins expressed on SiNW slides with the sameprinting pattern as above (not shown). Query DNA that encoded HA-taggedFOS was mixed in the IVTT lysate mixture and co-expressed with the arrayproteins. Antibodies to FOS or HA-tag were then used to reveal specificinteractions of FOS with JUN displayed on the array. The query proteinHA-FOS did not have the GST tag and could not be captured by anti-GSTantibody co-spotted in each well. HA-FOS would be detected only if theycould bind to the captured array target proteins tethered to the well.

Highly specific antibodies were selected for the interaction study. Ifno query DNAs were added to the expression system, anti-HA did notdetect any reactivity and anti-Fos only detected FOS spots on expressedarrays (not shown). The studies also further confirmed confinedexpression of FOS in individual wells on silicon nanowell arrays usingabove described vacuum assisted filling and sealing method, and showedspecific Fos-Jun interaction with HA-FOS protein as a query and detectedby an anti-Fos antibody. As antibodies against proteins of interest arenot always available, we also demonstrated detection of proteininteractions by using antibodies against the HA tag on the query protein(not shown).

Ultra-High Density Protein Arrays

To determine if the silicon nanowell platform is also compatible with ahuman proteome-on-chip scale, we produced two versions of ultra-highdensity arrays with 24,000 features. Displaying 24,000 proteins on asingle array requires nanowells with array spacing of 225 microns orbelow. 225 micron period silicon nanowells were produced in bothround-well and square-well geometries (FIG. 27). While the roundnanowells were produced using HNA etch chemistry, square nanowells wereproduced using KOH anisotropic etch chemistry on Si (100) wafers withwell-depth of approximately 100 microns. Etch anisotropy of square wellswhich produces deep wells with no significant lateral etching is ofinterest for further higher density protein arrays. Protein expressionand capture were tested in these chips using the standard protocol.Comparable signals were achieved on these 24,000 feature arrays relativeto those on the 8,000 feature arrays indicating robust proteinexpression on these ultra-high density arrays and relieving concerns ofpotential expression lysate exhaustion in smaller volume wells. Brightsignals along the edges of the square nanowells in FIG. 27 f arespeculated to be due to preferential aggregation of proteins and dye atthe sharp edges. Sequential KOH anisotropic etching followed byshort-duration HNA isotropic etching to round-off all the sharp edges isexpected to solve this issue. It is notable that even at this density,there was no significant cross-talk signal in neighboring wells in bothround and square nanowell geometries, confirming effective limiting ofdiffusion in sealed silicon nanowells compatible with proteome-on-chiptechnology.

Discussion

Establishing a platform to study protein biochemical properties in amultiplexed and high-throughput fashion is important for many differentbiomedical research areas. Protein microarrays represent one suchplatform. NAPPA is an innovative alternative to conventional proteinarrays and bypasses the challenges associated with protein expression,purification and storage. NAPPA is a particularly flexible proteinmicroarray format because a customized array can be created simply byre-arraying a series of plasmids encoding proteins of interest. However,transcription and translation on a planar surface entails the presenceof intermediates that can diffuse before capture by co-spotted capturereagent. Furthermore, planar surfaces are limited to assays that do nothave diffusible products or reactants that need to remain local.

In this study, we have developed a silicon nanowell based proteinmicroarray platform that not only addresses the cross-talk problem inhigh density NAPPA but also has the potential of performing otherbiochemical reactions in these nano-reaction vessels that are notpossible on traditional planar protein array format. For example, thekinetics of enzymatic assays that release fluorescent products might bemonitored directly in each well or various post-translationalmodifications could be performed on displayed proteins. Our NAPPA SiNWplatform builds upon the mature semi-conductor industry for substratemicro fabrication. Although most of our experiments used a density of8,000 features per standard glass slide with center-to-center distanceof 375 um, we do not foresee any obstacles of increasing densities manytimes higher and we have run proof-of-concept expression on arrays with24,000 features.

We have observed minor regional variations in signal intensities withinthe curved nanowells. These variations are also observed on flatsurfaces and probably represent non-uniform settling of precipitatesduring drying of microarray spots. Other contributors may includeincomplete filling of the nanowells during printing causing some signalattenuation towards the edges, and/or non-uniform surface irregularitiesdue to wet-etching of the nanowells.

Materials and Methods Micro Fabrication of Silicon Nanowells

Six inch diameter Silicon <100> wafers were used as starting materialfor producing silicon nanowell (SiNW) slides. Each 6-inch wafer yielded6 slides per wafer after dicing. In future, larger diameter wafers areexpected to yield higher number of slides per wafer, making SiNW slidesvery inexpensive. Standard semiconductor processing techniques were usedto fabricate the SiNW slides, as depicted in the schematic in FIG. 25.Silicon nanowell slides were fabricated at Arizona State UniversityCenter for Solid State Electronics Research. The wafers were firstcoated with 300 nm of LPCVD low stress nitride at 835 C, which acts as amask layer for wet etching of nanowells. Wafers were then spin-coatedwith 1 micron thick AZ 3312 positive photo resist (AZ ElectronicMaterials Inc), followed by soft bake on a hotplate at 100 C for 2minutes. Photo lithography masks with circular features were used toexpose the resist on an OAI photo mask aligner, for producing roundnanowells of desired diameter and spacing. The photo resist was thendeveloped in AZ300 MIF developer for 45 seconds, and hard-baked onhotplate at 100° C. for 2 minutes. Reactive ion etching using CHF₃—O₂plasma was used to etch away the nitride film, and open circular arraypattern on the nitride layer. Photo resist layer was washed away usingacetone.

Isotropic and Anisotropic Etching of Nanowells

Isotropic etching of wells was selected as preferred method compared toanisotropic etching. While anisotropic etching has the advantage ofproducing wells of high aspect ratio, it results in sharp facets andedges inside the nanowell. It was observed that piezo-dispensedDNA/plasmid mixture and the expressed proteins both tend to aggregateand bind preferentially at these sharp edges. To attain a relativelyuniform protein binding inside the wells a semi-spherical curved surfacewas produced using isotropic etching. Furthermore, etch mask and etchtime were designed so as to produce a circular flat surface at thebottom of the semi-sphere, which acts as a substrate for dispensedDNA/plasmid mixture. Flat circular surface at the bottom of thesemispherical wells has the advantage of distributing the dispensed DNAand the resulting protein binding, uniformly over the flat area,compared to a fully-spherical curved bottom which tends to aggregatethese into a spot at the center.

HNA silicon etchant was prepared by mixing hydrofluoric acid (49%),nitric acid (70%) and glacial acetic acid (98%) in the ratio of2.75:1.75:1. All chemicals were procured from Sigma Aldrich. HNA etchantis an extremely aggressive and corrosive mixture. It has to be preparedin special acid baths, and requires very careful handling with specialdisposal methods, by well trained personnel. HNA mixture etches siliconat an approximate rate of 3 microns per minute. 30 minute etch ofsilicon produced wells with depths ranging from 60 microns to 80microns, depending on diameter of the circular openings in thenitride-mask. Anisotropic pyramidal wells (FIG. 27 f, proof of concept225 micron period array) were produced by patterning square openings innitride mask layer on Si (1000) wafers, and etching in 30% KOH solutionat 80° C. Hot KOH is an aggressive chemical, strong corrosive, and needsto be handled by well-trained users. The sharp edges produced byanisotropic etching can be smoothed using a two-step process, with anHNA isotropic etch step following an anisotropic etch process.

Silicon surface at the bottom of the etched wells quenches fluorescentsignal during assay, query detection in later steps. Hence a thin filmof silicon dioxide was thermally grown that acts as a suitabledielectric and also mimics the glass surface of regular NAPPA arrays.For this purpose, wafers with etched wells were cleaned in Piranhamixture (1:1 mix of sulfuric acid and hydrogen peroxide) followed by aten second clean in buffered oxide etch (1:6 mixture of HF and NH₄F).Piranha mixture and buffered oxide etch are both very aggressivechemicals, to be prepared in special containers, and needs to be handledby well-trained users. A dry oxide of thickness 100 nm was thermallygrown at 1,000° C. in Tystar 4600 oxygen furnace. After oxide growth themask nitride film is etched away in hot phosphoric acid (185° C.). Theresultant wafers have round wells coated with uniform 100 nm oxide thinfilm, with spacing in-between wells comprising of semi-metallic siliconsurface. This structure has the additional advantage that fluorescentsignal is emitted from glass-like the oxide coated wells, while themetal-like silicon surface in un-etched areas in-between the wellsquenches any fluorescent emission (apparent in FIG. 26 d—no seal case),providing a good contrast in fluorescent imaging. Finally the waferswere diced into microscope-slide sizes yielding silicon nanowell (SiNW)substrates for high density NAPPA protein arrays.

Amine Functionalization of Silicon Dioxide Surface

Prior to piezo-dispensing of DNA/plasmid mixture into the nanowells thesurface of the wells was coated with amino-propyl-triethoxy-silane(APTES) monolayer. It has been demonstrated that for producing NAPPAprotein arrays, an amine terminated surface that acts as suitablesubstrate to adhere to dispensed DNA/plasmid mixture is required. Forthis purpose SiNW substrates were first cleaned in Piranha mixture (1:1H₂SO₄ and H₂O₂) for a period of 15 minutes. Piranha mix is a strongoxidant that cleans any residual organic materials on the SiNWsubstrates and oxidizes surface of silicon oxide to produce silanol(—SiOH) surface terminations. SiNW slides are then immersed in 2%solution of APTES in acetone, for a period of 15 minutes, followed bythorough rinse in acetone and DI water, to produce uniform monolayer ofAPTES molecules.

High Speed Piezo Printing in Nanowells

Piezo printing was accomplished using an au302 piezo dispense system(see web site engineeringarts.com) with a newly developed integratedalignment system for nanowell slides. The alignment system consists of amicrometer angular alignment fixture, look-down camera, transfer arm andvacuum tray. Nanowell slides are aligned one at a time on the alignmentfixture using the look down camera and then transferred with thetransfer arm to the vacuum tray. A row of aligned nanowell slides placedon the vacuum tray can then be dispensed “on-the-fly” with the headmoving at 175 mm/sec resulting in a peak speed of 50 wells per secondusing 8 dispense head. Each nanowell is filled with 800 picoliters ofprinting solution (cDNA+printing-mix). Following piezo printing of cDNAin nanowell array, NAPPA SiNW slides were stored in dry, sealedcontainer until the time of use.

DNA preparation Sequence-verified, full-length cDNA expression plasmidsin the T7-based mammalian expression vector pANT7_cGST or pANT7-nHA wereobtained from Arizona State University, Biodesign Institute, CenterPersonal Diagnostics, DNASU and are publicly available (see web sitednasu.asu.edu/DNASU/). The high-throughput preparation of high-qualitysupercoiled DNA for cell-free protein expression was performed asdescribed (30). For protein interaction assay, larger quantities ofquery DNA were prepared using standard Nucleobond preparation methods(Macherey-Nagel Inc., Bethlehem, Pa.).

Protein Expression

Protein display was performed as described (9). Displayed proteins weredetected using Tyramide signal amplification (TSA, Life technologies,Carlsbad, Calif.) with a monoclonal anti-GST antibody (Cell signalingInc., Danvers, Mass.) and HRP-labeled anti-mouse antibody (JacksonImmunoResearch, West Grove, Pa.). Anti-p53 monoclonal antibody (SantaCruz Biotechnology Santa Cruz, Calif.) was used for p53 specific signaldetection to assess diffusion.

Protein Interaction

Protein interaction was performed as described (9). FOS gene inpANT7-nHA was added to the RRL expression mixture at a concentration of1 ng/ml. HA-tagged FOS bound to interaction partners on array wasdetected either by gene specific anti-FOS (Santa Cruz Biotechnology,Santa Cruz, Calif.) antibody or tag specific antibody (anti-HA,Convance) followed by Alexa fluor labeled secondary antibodies (Lifetechnologies, Carlsbad, Calif.).

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The present invention is illustrated by way of the foregoing descriptionand examples. The foregoing description is intended as a non-limitingillustration, since many variations will become apparent to thoseskilled in the art in view thereof. It is intended that all suchvariations within the scope and spirit of the appended claims beembraced thereby. Each referenced document herein is incorporated byreference in its entirety for all purposes. Changes can be made in thecomposition, operation and arrangement of the method of the presentinvention described herein without departing from the concept and scopeof the invention as defined herein.

1. A biomolecule array, comprising (a) a first substrate; and (b)biomolecules comprising at least 10 isolated coding nucleic acids and/orat least 10 isolated polypeptides, wherein each nucleic acid and/orpolypeptide is physically confined at a discrete location on the firstsubstrate, and wherein each nucleic acid is capable of expressing itsencoded product in situ at its discrete location on the substrate,and/or wherein each polypeptide is capable of a characteristic activityin situ at its discrete location on the substrate; wherein the discretelocations are separated from each other on the first substrate by acenter to center spacing of between about 20 nm and about 1 mm.
 2. Thebiomolecule array of claim 1, wherein the discrete locations areseparated from each other on the first substrate by a center to centerspacing of between about 20 nm and about 100 μm.
 3. The biomoleculearray of claim 1, wherein each physically confined discrete locationcomprises a well.
 4. The biomolecule array of claim 3, wherein each wellhas a diameter of between about 14 nm and about 0.75 mm.
 5. Thebiomolecule array of claim 3, wherein the wells are present on the firstsubstrate at a density of between about 250 billion wells per squarecentimeter and about 100 wells per square centimeter.
 6. (canceled) 7.The biomolecule array of claim 1, wherein each discrete location furthercomprises reagents for expressing the encoded nucleic acid productand/or for testing polypeptide activity.
 8. The biomolecule array ofclaim 1, wherein each discrete location further comprises reagents forexpressing the encoded nucleic acid product and/or for testingpolypeptide activity and where those reagents are added to the arrayseparately from the nucleic acids or polypeptides.
 9. The biomoleculearray of claim 8, wherein the reagent comprises a reticulocyte lysate.10. The biomolecule array of claim 9, wherein the biomolecules compriseat least 100 isolated coding nucleic acids.
 11. (canceled)
 12. Thebiomolecule array of claim 1, wherein the biomolecules comprise at least100 isolated polypeptides.
 13. The biomolecule array of claim 1, whereinthe nucleic acids and/or polypeptides are bound to the substrate. 14.The biomolecule array of claim 1, wherein either (i) the array furthercomprises a capture substrate adapted to mate with the first substratewherein the capture substrate is functionalized to capture and isolatethe expression product; or (ii) the discrete locations are furtherfunctionalized to capture and isolate the expression product.
 15. Anarray comprising (a) a silicon-containing substrate, having a surfacecomprising a plurality of nanowells at discrete locations wherein thediscrete locations are separated from each other on thesilicon-containing substrate by a center to center spacing of betweenabout 20 nm and about 1 mm; and (b) biomolecules capable of capturinganother molecule located at each discrete location.
 16. The array ofclaim 15, wherein the discrete locations are separated from each otheron the first substrate by a center to center spacing of between about 20nm and about 100 μm.
 17. The array of claim 15, wherein the biomoleculescomprise antigen or antibodies, and the like.
 18. (canceled) 19.(canceled)
 20. (canceled)
 21. (canceled)
 22. The array of claim 15wherein the wells are sealed by a mating substrate.
 23. A method for insitu nucleic acid expression, comprising (a) contacting each discretelocation of the array of claim 1 with reagents for nucleic acidexpression to form a mixture; and (b) incubating the mixture underconditions suitable for nucleic acid expression.
 24. A method forexpressing and capturing a product, comprising (a) contacting a nucleicacid array with reagents for nucleic acid expression to form a mixture,wherein the nucleic acid array comprises a first substrate and at least10 isolated coding nucleic acids physically confined at a discretelocation on a first substrate, and wherein each nucleic acid is capableof expressing its encoded product in situ at its discrete location onthe first substrate; (b) optionally, bringing the first substrate intothe proximity of a capture substrate; (c) incubating the mixture underconditions suitable for production of nucleic acid expression products;and (d) capturing and isolating the expression products on the firstsubstrate or, when present, the capture substrate.
 25. The method ofclaim 24, wherein the capture substrate comprises a second substratethat comprises a plurality of physically confined discrete locationsthat match the physically confined discrete locations on the firstsubstrate.
 26. The method of claim 24, wherein the method comprisesprecoating the first substrate or the capture substrate, when present,with a first member of a binding pair, wherein the expression productscomprise a second member of the binding pair, and wherein the incubatingis done under conditions suitable for binding of the first member andthe second member of the binding pair, resulting in capture of theexpression product on the precoated substrate.
 27. (canceled) 28.(canceled)
 29. (canceled)
 30. (canceled)
 31. (canceled)
 32. (canceled)33. (canceled)
 34. (canceled)
 35. (canceled)
 36. (canceled)